the basics of essential documents in the trial master file – part 2 - during the clinical conduct
Published 7 months ago • 1.8K plays • Length 5:55Download video MP4
Download video MP3
Similar videos
-
8:53
the basics of essential documents in the trial master file – part 1 - before the clinical phase
-
5:18
the basics of essential documents in the trial master file – part 3 - after the clinical phase
-
9:30
clinical trials in the netherlands and belgium - part 1
-
5:54
basics - part 22 - essential documents
-
4:40
basics - part 21 - jobs in clinical trials: trial master file manager
-
8:48
clinical research job interview tips and strategies
-
42:49
gcp-mindset: daily life of a cra
-
3:44
clinical research mock interview conducted by cliniminds
-
5:58
good clinical practice and ich gcp guidelines
-
5:25
understanding the basics: data management in clinical research
-
5:18
rule 6 of the responsibilities of the investigator according to gcp
-
3:12
basics - part 28 - the trial site
-
5:25
cra basics: vendor management in clinical research
-
11:03
the 13 principles of good clinical practice (gcp) - part 2 of 2
-
8:18
what is document management in clinical research?
-
5:39
rule 2 of the responsibilities of the investigator according to gcp
-
7:01
cra basics: understanding the role of biomarkers in clinical trials
-
8:03
cra basics: good to know about visits - pre-study visit psv - part 2
-
3:33
the audit in the clinical trial - part 1
-
3:37
what is the alcoa principle?
-
4:35
what everybody should know about clinical trials! - part 2 - medical device legislation